HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037995Generated: October 31, 2026
Ethyl acetate hexane → HCID 178514971, compound
https://huagongshe.com/reaction/1037995
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | 1H-Indazole-1-carboxylic acid, 3-(bromomethyl)-5-nitro-, 1,1-dimethylethyl ester | HCID 57686130 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 178514971 | HCID 178514971 | — |
Reaction Steps
3-Bromomethyl-5-nitro-indazole-1-carboxylic acid tert-butyl ester (0.63 g, 1.77 mmol) and potassium phthalimide (0.396 g, 1.2 eq) were stirred in DMF (1 mL) at 80° C. for two hours. TLC (20% EtOAc/hexane) showed starting material consumed and new products formed. After DMF was evaporated, a residue, 1.33 g, was obtained. The resulting residue was stirred in DCM and filtered. The filtration cake then washed with DCM followed by hexane. The evaporation of the filtrate gave 0.79 g of crude. Flash chromatograph (20-30% EtOAc/hexane) gave a mixture, two spots shown on TLC. During the sample preparation, solid precipitated and the solid was collected, 95 mg. MS showed de-Boc product, (M+H)+ at 323. An adequate amount of this mixture was treated with TFA in DCM for two hours. TLC showed one spot and MS gave (M+H)+ at 323. The remaining mixture was stirred in a mixture of TFA (6 mL) and DCM (10 mL) for two hours. Evaporation of TFA and DCM gave the desired product, 0.71 g, (quant. yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546404B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-bf62197c840943c29fa672fda92842a1 |
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| Source note | uspto-grants-2013_10 |
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